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33 diagnostice diferențiale pentru hypotrichosis

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  • Sindromul Hoyeraal-Hreidarsson

    […] and recurrent skin vesicles ; 613102 ; DSC3 Hypotrichosis simplex of scalp ; 146520 ; CDSN Hypotrichosis, congenital, with juvenile macular dystrophy ; 601553 ; CDH3 Hypotrichosis[epo.wikitrans.net] […] narrowed the potential location to an 11.4-Mb interval on chromosome Xq25-27; however, the causative gene remains unknown.[ 138 ] Characteristic physical findings include hypotrichosis[theola.yokarialba.com] , hereditary, Marie Unna type, 1 ; 146550 ; HR Hypotrichosis, localized, autosomal recessive 2 ; 604379 ; LIPH Hypotrichosis, localized, autosomal recessive, 3 ; 611452 ;[epo.wikitrans.net]

  • Sindromul Strudwick

    […] and recurrent skin vesicles ; 613102 ; DSC3 Hypotrichosis simplex of scalp ; 146520 ; CDSN Hypotrichosis, congenital, with juvenile macular dystrophy ; 601553 ; CDH3 Hypotrichosis[epo.wikitrans.net] White (183,849, a): hypotrichosis kongjenitale, Rizomelicheskaya stunting, kufizim hip rrëmbimin, metaphysis zgjeruar, kockëzim e prishjes terren epiphysis vonesë në metaphysis[kingad.ru] , hereditary, Marie Unna type, 1 ; 146550 ; HR Hypotrichosis, localized, autosomal recessive 2 ; 604379 ; LIPH Hypotrichosis, localized, autosomal recessive, 3 ; 611452 ;[epo.wikitrans.net]

  • Bradiopsia

    […] deficit, Lopes type Hypotrichosis-intellectual deficit, Lopes type Idiopathic hydrops fetalis Idiopathic short stature Idiopathic short stature Imperforate oropharynx - costo[happylibnet.com] Doença de Charcot-Marie-Tooth tipo B, 254334 intermédia, autossómica recessiva 250977 Ribosiduria-AICA 300536 CDG syndrome type IR 1 Caso 324422 ALG13-CDG syndrome 330029 Hypotrichosis-deafness[kipdf.com] […] doenças Prevalência estimada (/100,000) Hypopigmentation-punctate 324561 palmoplantar keratoderma syndrome Hypotonia-cerebral atrophy363424 hyperglycinemia syndrome 330029 Hypotrichosis-deafness[doczz.com.br]

  • Sindromul Weissenbacher-Zweymuller

    […] and recurrent skin vesicles ; 613102 ; DSC3 Hypotrichosis simplex of scalp ; 146520 ; CDSN Hypotrichosis, congenital, with juvenile macular dystrophy ; 601553 ; CDH3 Hypotrichosis[epo.wikitrans.net] , hereditary, Marie Unna type, 1 ; 146550 ; HR Hypotrichosis, localized, autosomal recessive 2 ; 604379 ; LIPH Hypotrichosis, localized, autosomal recessive, 3 ; 611452 ;[epo.wikitrans.net] P2RY5 Hypotrichosis, localized, autosomal recessive ; 607903 ; DSG4 Hypotrichosis-lymphedema-telangiectasia syndrome ; 607823 ; SOX18 Hypouricemia, renal, 2 ; 612076 ; SLC2A9[epo.wikitrans.net]

  • Sindromul Gorlin

    […] este ektomezodermalnaya ereditară-familială) boală ereditară, manifestată prin formarea de focare brusc demarcate subțierea pielii hiperpigmentate, unghiilor distrofie, hypotrichosis[ro.detailabout.com]

  • Sindromul Sorsby

    […] and recurrent skin vesicles ; 613102 ; DSC3 Hypotrichosis simplex of scalp ; 146520 ; CDSN Hypotrichosis, congenital, with juvenile macular dystrophy ; 601553 ; CDH3 Hypotrichosis[epo.wikitrans.net] , hereditary, Marie Unna type, 1 ; 146550 ; HR Hypotrichosis, localized, autosomal recessive 2 ; 604379 ; LIPH Hypotrichosis, localized, autosomal recessive, 3 ; 611452 ;[epo.wikitrans.net] P2RY5 Hypotrichosis, localized, autosomal recessive ; 607903 ; DSG4 Hypotrichosis-lymphedema-telangiectasia syndrome ; 607823 ; SOX18 Hypouricemia, renal, 2 ; 612076 ; SLC2A9[epo.wikitrans.net]

  • Hiperkeratoza palmară și plantară

    Clinical aspects included as follows: liniar ichtyosis Comel, atopic eczema and trichodystrophy (hypotrichosis and trichorrhexis invaginata).[old.library.usmf.md]

  • Vitreoretinopatie exudativă familială

    […] deficit, Lopes type Hypotrichosis-intellectual deficit, Lopes type Idiopathic hydrops fetalis Idiopathic short stature Idiopathic short stature Imperforate oropharynx - costo[happylibnet.com] Metaphyseal dysplasia without hypotrichosis Metaphyseal dysplasia, Braun-Tinschert type Metatropic dysplasia type 1 Metatropic dysplasia type 1 Michels syndrome Michels syndrome[happylibnet.com] , Spahr type Metaphyseal dysostosis - intellectual deficit - conductive deafness Metaphyseal dysplasia - maxillary hypoplasia - brachydacty Metaphyseal dysplasia without hypotrichosis[happylibnet.com]

  • Limfadenita tuberculoasă cervicală

    (tiamina) Vitamina B2 Hypovitaminoza (Riboflavina) Vitamina B3 Hipovitaminoza (vitamina PP) Vitamina B6 Hipovitaminoza (piridoxina) Vitamina E Hipovitaminoza (tocoferol) hypotrichosis[fmedical.ru]

  • Sindromul Jaffe-Campanacci

    Hypotrichosis-lymphedema-telangiectasia sindromo Ichthyosis-fragila harar-difektita inteligentec-malkreskinta fekundec-manka statursindromo (IBIDS-sindromo, sulfur-mankhava[epo.wikitrans.net] […] skleroziĝadpoikiloderma Heterochromia iridum Holocarboxylase-sintetaseomanko Hipohidrota ektoderma displazio (anhidrota ektoderma displazio, Christ-Siemens-Touraine-sindromo) Hypotrichosis-acro-osteolysis-onychogryphosis-palmoplantar-keratoderma-periodontitsindromo[epo.wikitrans.net]

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